Arizona Sun Sunscreen SPF 8
- Product NDC
- 61973-113
- 11-digit product format
- 619730113
- Labeler code
- 61973
- Product ID
- 61973-113_4f0be9a2-5641-baaf-e063-6394a90a0f5b
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Sunscreen
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- Arizona Sun Products
- Application
- M020
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2024-02-21
- Substance
- AVOBENZONE; OCTINOXATE; OCTISALATE; OXYBENZONE
- Active strength
- 10; 65; 10; 10 mg/g; mg/g; mg/g; mg/g
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Arizona Sun Sunscreen SPF 8
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| AVOBENZONE | 10 mg/g |
| OCTINOXATE | 65 mg/g |
| OCTISALATE | 10 mg/g |
| OXYBENZONE | 10 mg/g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | G63QQF2NOX, 4Y5P7MUD51, 4X49Y0596W, 95OOS7VE0Y |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 61973-113-01 | Arizona Sun Sunscreen SPF 8 | 30 g in 1 BOTTLE | LOTION | 30 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 61973-113 | ARIZONA SUN SUNSCREEN SPF 8 (SUNSCREEN) LOTION [ARIZONA SUN PRODUCTS] | 2 | Current NDC | 20240308_106a9608-f7a4-0f8c-e063-6394a90a26ab.zip |
| 61973-113 | ARIZONA SUN SUNSCREEN SPF 8 (SUNSCREEN) LOTION [ARIZONA SUN PRODUCTS] | 1 | Current NDC, 1 package rows | 20240308_11e8b612-29be-47ed-e063-6394a90ab9e7.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 61973-113-01 | 61973011301 | 30 g in 1 BOTTLE (61973-113-01) | 30 g | 2024-02-21 | No | No | Current |